ClearanceBrief
510(k) K190536 ยท JXE Device, Nerve Conduction Velocity Measurement

Mediracer NCS

ApplicantMediracer OY, Oulu, FI
DecisionSubstantially Equivalent, Sep 25, 2019
ReceivedMar 4, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190536

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.